Other search tools

About this data

The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

If you have any questions or comments, please contact us.

Results: 1 to 1 of 1

Publication Record

Connections

Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome).
Coldren CD, Lai Z, Shragg P, Rossi E, Glidewell SC, Zuffardi O, Mattina T, Ivy DD, Curfs LM, Mattson SN, Riley EP, Treier M, Grossfeld PD
(2009) Neurogenetics 10: 89-95
MeSH Terms: Adolescent, Adult, Animals, Child, Chromosome Deletion, Chromosome Mapping, Chromosomes, Human, Pair 11, Cognition Disorders, Female, Homeodomain Proteins, Humans, Jacobsen Distal 11q Deletion Syndrome, Male, Mental Disorders, Mice, Microarray Analysis, Nerve Tissue Proteins, Neurogranin, Prospective Studies, Young Adult
Added November 17, 2011
0 Communities
1 Members
0 Resources
20 MeSH Terms